ClinVar Miner

List of variants reported as likely benign for Wilms tumor type 1

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_004484.3(GPC3):c.1032+10_1032+11delinsTT rs1556297529
NM_004484.3(GPC3):c.1212T>C (p.Ala404=) rs1556263726
NM_004484.3(GPC3):c.1686G>C (p.Leu562=) rs1556111740
NM_004484.3(GPC3):c.1737G>A (p.Val579=) rs1556111517
NM_004484.3(GPC3):c.338-4A>T rs1490568896
NM_004484.3(GPC3):c.384C>A (p.Ala128=) rs761541528
NM_024426.6(WT1):c.1143G>A (p.Pro381=) rs1554939849
NM_024426.6(WT1):c.1227G>A (p.Lys409=) rs1554939791
NM_024426.6(WT1):c.1260C>T (p.His420=) rs1554939784
NM_024426.6(WT1):c.1341A>G (p.Gln447=) rs772822466
NM_024426.6(WT1):c.1422C>T (p.His474=) rs1554939066
NM_024426.6(WT1):c.1479T>C (p.Ser493=) rs1334930117
NM_024426.6(WT1):c.150C>T (p.Ala50=) rs1554946724
NM_024426.6(WT1):c.1515C>A (p.Val505=) rs1338629886
NM_024426.6(WT1):c.216G>T (p.Gln72His) rs5030135
NM_024426.6(WT1):c.315G>A (p.Ala105=) rs1554946607
NM_024426.6(WT1):c.381C>T (p.Pro127=) rs771681406
NM_024426.6(WT1):c.42C>T (p.Val14=) rs1343194102
NM_024426.6(WT1):c.450C>T (p.Ser150=) rs1213710686
NM_024426.6(WT1):c.480G>A (p.Gln160=) rs758900425
NM_024426.6(WT1):c.498T>C (p.Thr166=) rs1554946487
NM_024426.6(WT1):c.555C>T (p.Phe185=) rs1554946465
NM_024426.6(WT1):c.585C>T (p.Ser195=) rs1332888095
NM_024426.6(WT1):c.633C>T (p.Leu211=) rs576677344
NM_024426.6(WT1):c.662-10G>T rs1554945255
NM_024426.6(WT1):c.662-6C>A rs372418954
NM_024426.6(WT1):c.672G>A (p.Thr224=) rs756695525
NM_024426.6(WT1):c.726G>T (p.Ala242=) rs1473494675
NM_024426.6(WT1):c.75C>T (p.Ser25=) rs1417997475
NM_024426.6(WT1):c.784+10C>A rs1554945172
NM_024426.6(WT1):c.87C>T (p.Cys29=) rs1554946770
NM_024426.6(WT1):c.966-4del rs1438888966

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